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Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative
Scutellarin (1) has been widely used to treat acute cerebral infarction in clinic, but poor aqueous solubility decreases its bioavailability. Interestingly, scutellarin (1) could be metabolized into scutellarein (2) in vivo. In this study, a sulfonic group was introduced at position C-8 of scutellar...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152701/ https://www.ncbi.nlm.nih.gov/pubmed/28635646 http://dx.doi.org/10.3390/molecules22061028 |
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author | Gu, Ting Zhong, Yue Lu, Yu-Ting Sun, Ying Dong, Ze-Xi Wu, Wen-Yu Shi, Zhi-Hao Li, Nian-Guang Xue, Xin Fang, Fang Li, He-Min Tang, Yu-Ping |
author_facet | Gu, Ting Zhong, Yue Lu, Yu-Ting Sun, Ying Dong, Ze-Xi Wu, Wen-Yu Shi, Zhi-Hao Li, Nian-Guang Xue, Xin Fang, Fang Li, He-Min Tang, Yu-Ping |
author_sort | Gu, Ting |
collection | PubMed |
description | Scutellarin (1) has been widely used to treat acute cerebral infarction in clinic, but poor aqueous solubility decreases its bioavailability. Interestingly, scutellarin (1) could be metabolized into scutellarein (2) in vivo. In this study, a sulfonic group was introduced at position C-8 of scutellarein (2) to enhance the aqueous solubility of the obtained derivative (3). DPPH (1,1-diphenyl-2-picrylhydrazyl)-radical scavenging ability and antithrombic activity were also conducted to determine its bioactivity. The result showed that scutellarein derivate (3) could be a better agent for ischemic cerebrovascular disease treatment. |
format | Online Article Text |
id | pubmed-6152701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61527012018-11-13 Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative Gu, Ting Zhong, Yue Lu, Yu-Ting Sun, Ying Dong, Ze-Xi Wu, Wen-Yu Shi, Zhi-Hao Li, Nian-Guang Xue, Xin Fang, Fang Li, He-Min Tang, Yu-Ping Molecules Article Scutellarin (1) has been widely used to treat acute cerebral infarction in clinic, but poor aqueous solubility decreases its bioavailability. Interestingly, scutellarin (1) could be metabolized into scutellarein (2) in vivo. In this study, a sulfonic group was introduced at position C-8 of scutellarein (2) to enhance the aqueous solubility of the obtained derivative (3). DPPH (1,1-diphenyl-2-picrylhydrazyl)-radical scavenging ability and antithrombic activity were also conducted to determine its bioactivity. The result showed that scutellarein derivate (3) could be a better agent for ischemic cerebrovascular disease treatment. MDPI 2017-06-21 /pmc/articles/PMC6152701/ /pubmed/28635646 http://dx.doi.org/10.3390/molecules22061028 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gu, Ting Zhong, Yue Lu, Yu-Ting Sun, Ying Dong, Ze-Xi Wu, Wen-Yu Shi, Zhi-Hao Li, Nian-Guang Xue, Xin Fang, Fang Li, He-Min Tang, Yu-Ping Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative |
title | Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative |
title_full | Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative |
title_fullStr | Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative |
title_full_unstemmed | Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative |
title_short | Synthesis and Bioactivity Characterization of Scutellarein Sulfonated Derivative |
title_sort | synthesis and bioactivity characterization of scutellarein sulfonated derivative |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152701/ https://www.ncbi.nlm.nih.gov/pubmed/28635646 http://dx.doi.org/10.3390/molecules22061028 |
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